| Literature DB >> 33427200 |
Luke M Noble1,2, John Yuen1, Lewis Stevens3, Nicolas Moya3, Riaad Persaud1, Marc Moscatelli1, Jacqueline L Jackson1, Gaotian Zhang3, Rojin Chitrakar4, L Ryan Baugh4, Christian Braendle5, Erik C Andersen3, Hannah S Seidel6, Matthew V Rockman1.
Abstract
Mating systems have profound effects on genetic diversity and compatibility. The convergent evolution of self-fertilization in three Caenorhabditis species provides a powerful lens to examine causes and consequences of mating system transitions. Among the selfers, Caenorhabditis tropicalis is the least genetically diverse and most afflicted by outbreeding depression. We generated a chromosomal-scale genome for C. tropicalis and surveyed global diversity. Population structure is very strong, and islands of extreme divergence punctuate a genomic background that is highly homogeneous around the globe. Outbreeding depression in the laboratory is caused largely by multiple Medea-like elements, genetically consistent with maternal toxin/zygotic antidote systems. Loci with Medea activity harbor novel and duplicated genes, and their activity is modified by mito-nuclear background. Segregating Medea elements dramatically reduce fitness, and simulations show that selfing limits their spread. Frequent selfing in C. tropicalis may therefore be a strategy to avoid Medea-mediated outbreeding depression.Entities:
Keywords: C. elegans; balancing selection; caenorhabditis tropicalis; evolutionary biology; gene drive; genetics; genomics; mating systems; population genetics; selfing
Mesh:
Year: 2021 PMID: 33427200 PMCID: PMC7853720 DOI: 10.7554/eLife.62587
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140